Safety and Tolerability Study of Liquid Alpha1 Proteinase Inhibitor (API) in Subjects With Cystic Fibrosis
- Conditions
- Cystic Fibrosis
- Interventions
- Biological: CR002 Liquid APIBiological: Placebo
- Registration Number
- NCT01347190
- Lead Sponsor
- CSL Behring
- Brief Summary
Study to assess safety and tolerability of a single dose of study-drug administered to Cystic Fibrosis (CF) patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 25
-
Have a confirmed diagnosis of CF: one or more clinical findings consistent with CF and at least one of the following:
- Sweat chloride ≥ 60 mEq/L by quantitative pilocarpine iontophoresis test OR
- A genotype with two identifiable mutations consistent with CF (∆F508 homozygous or two alleles known to cause a class I, II, or III mutation)
-
Have an FEV1 ≥30% of predicted normal as defined by age, gender, and height
- Oxygen saturation <90%
- Changed in treatment regimen within 2 weeks prior to screening
- Antibiotics regimen change < 4 weeks before screening
- Persistent colonization with Burkholderia cepacia
- Serum IgA < 50% of lower level of normal
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Liquid API CR002 Liquid API - Placebo Placebo -
- Primary Outcome Measures
Name Time Method Frequency of Adverse events 44 Days (Day -21 to Day 22)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (11)
Site 20
🇵🇱Rabka Zdroj, Poland
Site 24
🇵🇱Bialystok, Poland
Site 11
🇧🇬Sofia, Bulgaria
Site 12
🇧🇬Varna, Bulgaria
Site 30
🇭🇺Debrecen, Hungary
Site 41
🇬🇧Southampton, United Kingdom
Site 21
🇵🇱Poznan, Poland
Site 22
🇵🇱Gdansk, Poland
Site 42
🇬🇧Papworth Hospital, United Kingdom
Site 40
🇬🇧Penarth, United Kingdom
Site 23
🇵🇱Warszawa, Poland